期刊
BIOLOGICAL PSYCHIATRY
卷 80, 期 1, 页码 40-52出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/j.biopsych.2015.05.014
关键词
Inflammation; Insomnia; Interleukin-6; Meta-analysis; Sleep deprivation; Sleep disturbance; Sleep duration
资金
- National Institute on Aging [R01-AG034588]
- National Institutes of Health [R01-CA119159, R01-HL079955, R01 HL095799, P30-AG028748, P30-AG017265, UL RR 033176]
- Cousins Center for Psychoneuroimmunology
- UCLA Claude D. Pepper Older Americans Independence Center
BACKGROUND: Sleep disturbance is associated with inflammatory disease risk and all-cause mortality. Here, we assess global evidence linking sleep disturbance, sleep duration, and inflammation in adult humans. METHODS: A systematic search of English language publications was performed, with inclusion of primary research articles that characterized sleep disturbance and/or sleep duration or performed experimental sleep deprivation and assessed inflammation by levels of circulating markers. Effect sizes (ES) and 95% confidence intervals (CI) were extracted and pooled using a random effect model. RESULTS: A total of 72 studies (n > 50,000) were analyzed with assessment of C-reactive protein (CRP), interleukin-6 (IL-6), and tumor necrosis factor alpha (TNF alpha). Sleep disturbance was associated with higher levels of CRP (ES .12; 95% CI = .05-.19) and IL-6 (ES .20; 95% CI = .08-.31). Shorter sleep duration, but not the extreme of short sleep, was associated with higher levels of CRP (ES .09; 95% CI = .01-.17) but not IL-6 (ES .03; 95% CI: -.09 to .14). The extreme of long sleep duration was associated with higher levels of CRP (ES .17; 95% CI = .01-.34) and IL-6 (ES .11; 95% CI = .02-20). Neither sleep disturbances nor sleep duration was associated with TNF alpha. Neither experimental sleep deprivation nor sleep restriction was associated with CRP, IL-6, or TNF alpha. Some heterogeneity among studies was found, but there was no evidence of publication bias. CONCLUSIONS: Sleep disturbance and long sleep duration, but not short sleep duration, are associated with increases in markers of systemic inflammation.
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